RGD:150332026 Rat Genome Database

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Variant: RGD:150332026 -  Homo sapiens

RGD ID: 150332026
RS ID: rs8193019
ClinVar ID: CV1169316
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CEL  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 135,939,976
GRCh38 9 133,064,589
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001807.6:c.217+35G>A
NG_016394.1:g.7612G>A
NC_000009.12:g.133064589G>A
NC_000009.11:g.135939976G>A
 07/10/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CEL
Accession:NM_001807
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001536724 CLINVAR
dbSNP (RS) rs8193019 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CEL CLINVAR
OMIM 114840 CLINVAR